Benefiber Prebiotic Fiber Supplement — Class II food recall F-0951-2020
Terminated recall by Glaxosmithkline Consumer Healthcare Holdings, reported 2020-05-13, distributed in AR, CA, FL, HI, ID, IL, LA, MA…. Fiber prebiotic product potentially contaminated with small plastic pieces
| Recall number | F-0951-2020 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Glaxosmithkline Consumer Healthcare Holdings, Warren, NJ, United States |
| Recall initiated | 2020-04-28 |
| Classified | 2020-05-18 |
| Reported by FDA | 2020-05-13 |
| Terminated | 2021-06-01 |
| Distributed | AR, CA, FL, HI, ID, IL, LA, MA, ME, MI, MN, MO, NC, NE, NJ, NY, OH, OR, PA, RI, SC, TX, VA, WA, WI |
| Quantity | 170,340 bottles |
| Reason classes | foreign material |
| UPC / GTIN / UDI-DI | 00886790218302 |
| Lot numbers | YT2Y |
| Expiration dates | 2021-10-20, 2021-11-20 |
Product
Benefiber Prebiotic Fiber Supplement, packaged in the following ways 1) Net Wt. 500 g (17.6 oz) bottle. UPC 886790218302 and 2) Net Wt. 760 g bottle UPC 8886790211907
Reason for recall
Fiber prebiotic product potentially contaminated with small plastic pieces
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-0951-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.